A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036279



Internal ID19125498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15876551..15889061hg38UCSC Ensembl
Innerchr10:15918550..15931060hg19UCSC Ensembl
Innerchr10:15958556..15971066hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3812511
hg1912511
hg1812511
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3514427, nssv3522286, nssv3516905
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036279
Frequency
Sample Size11257
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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